IBA (Ion Beam Applications)

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Description

6 dispositivos en la base de datos

  • Modelo / Serial
    Model Number: Proteus 235 Serial Number: PAT.003 (KR), PAT.006 (US), PAT.107 (DE), PAT.108 (US), PAT.109 (US), PAT.110 (US), PAT.111 (FR), PAT.113 (US), PAT.114 (CZ), PAT.115 (IT), SAT.116 (US), SAT.120 (DE), SAT.126 (US), SAT.132 (NL).
  • Descripción del producto
    Medical devices for diagnostics and radiation therapy
  • Modelo / Serial
    Model Number: Proteus 235 Serial Number: PAT.000 (US), PAT.001 (CN), PAT.003 (KR), PAT.006 (US), PAT.107 (EU), PAT.108 (US), PAT.109 (US), PAT.110 (US), PAT.111 (EU), PAT.112 (US), PAT.113 (US), PAT.114 (EU), PAT.115 (EU), SAT.116 (US), SAT.117 (EU), SAT.119 (US), SAT.120 (EU), SAT.122 (EU), SAT.123 (US), SAT.126 (US), SAT.132 (EU), SAT.133 (US), SBF.101 (EU), SBF.105 (US)
  • Descripción del producto
    Medical devices for diagnostics and radiation therapy
  • Modelo / Serial
    Catalog Number: Proteus 235 Model Number: Proteus 235 Serial Number: PAT.107, PAT.111, PAT.114, PAT.115, SAT.117, SAT.120, SAT.122
  • Descripción del producto
    Medical devices for diagnostics and radiation therapy
  • Modelo / Serial
    Model Number: Proteus ONE a Proteus PLUS (Proteus 235) a adaPT insight (I2C) Serial Number: PAT.000, PAT.003, PAT.006, PAT.107, PAT.108, PAT.109, PAT.110, PAT.111, PAT.112, PAT.113, PAT.114, PAT.115, SAT.116, SAT.117, SAT.119, SAT.120, SAT.122, SAT.123, SAT.126, SBF.101
  • Descripción del producto
    Medical devices for diagnostics and radiation therapy
  • Modelo / Serial
    Catalog Number: Proteus 235 Model Number: Proteus 235 Serial Number: EU: PAT.107 (Germany), PAT.111 (France) (the Device Mfr Date below corresponds to the delivery of PAT.111 IBA Proton Therapy site, first site delivered in European Union), PAT.114 (Czech Republic), PAT.115 (Italy), SAT.117 (Poland), SAT.120 (Germany), SAT.122 (Sweden). US: PAT.006, PAT.108, PAT.109, PAT.110, PAT.112, PAT.113, SAT.116, SAT.119, SAT.123, SAT.126. Korea: PAT.003.
  • Descripción del producto
    Medical devices for diagnostics and radiation therapy
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Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ